Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1654-2014 — ADVIA Centaur Systems TSH3 Ultra , Ready Pack, 500 test Catalog Number: 06491080; Siemens Material Number: 10282379. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.

U.S. FDA — Device Enforcement · United States · 2014-04-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1654-2014
Date of alert
2014-04-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
06491080
Reported risk: Samples containing fluorescein may show interference with the ADVIA Centaur¿ Systems TSH3 Ultra, Vitamin D and the ADVIA Centaur BRAHMS Procalcitonin assays.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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